Wang Zhenguo, Yang Jifei, Niu Qingli, Brayton Kelly A, Luo Jianxun, Liu Guangyuan, Yin Hong, Liu Zhijie
State Key Laboratory of Veterinary Etiological Biology, Key Laboratory of Veterinary Parasitology of Gansu Province, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, People's Republic of China.
Department of Veterinary Microbiology and Pathology, Washington State University, Pullman, WA, 99164, USA.
Parasit Vectors. 2017 Jul 28;10(1):359. doi: 10.1186/s13071-017-2297-z.
Ovine anaplasmosis is a tick-borne disease that is caused by Anaplasma ovis in sheep and goats. The pathogen is widely distributed in tropical and subtropical regions of the world. At present, diagnosis of the disease mainly depends on microscopy or nucleic acid based molecular tests, although a few serological tests have been applied for the detection of A. ovis infection.
Here we describe the identification of an A. ovis protein that is homologous to the A. marginale appendage-associated protein (AAAP). We expressed a recombinant fragment of this protein for the development of an indirect enzyme-linked immunosorbent assay (ELISA) for the detection of A. ovis. Anaplasma ovis-positive serum showed specific reactivity to recombinantly expressed AAAP (rAAAP), which was further confirmed by the rAAAP ELISA, which also demonstrated no cross-reactivity with sera from animals infected with A. bovis or other related pathogens in sheep and goats. Testing antibody kinetics of five experimentally infected sheep for 1 year demonstrated that the rAAAP ELISA is suitable for the detection of early and persistent infection of A. ovis infections. Investigation of 3138 field-collected serum samples from 54 regions in 23 provinces in China demonstrated that the seroprevalence varied from 9.4% to 65.3%, which is in agreement with previous reports of A. ovis infection.
An A. ovis derived antigenic protein, AAAP, was identified and the antigenicity of the recombinant AAAP was confirmed. Using rAAAP an indirect ELISA assay was established, and the assay has been proven to be an alternative serological diagnostic tool for investigating the prevalence of ovine anaplasmosis of sheep and goats.
绵羊无形体病是一种由绵羊无形体引起的蜱传疾病,主要感染绵羊和山羊。该病原体广泛分布于世界热带和亚热带地区。目前,该病的诊断主要依靠显微镜检查或基于核酸的分子检测,尽管也有一些血清学检测方法用于检测绵羊无形体感染。
在此,我们描述了一种与边缘无形体附属物相关蛋白(AAAP)同源的绵羊无形体蛋白的鉴定。我们表达了该蛋白的重组片段,用于开发检测绵羊无形体的间接酶联免疫吸附测定(ELISA)。绵羊无形体阳性血清对重组表达的AAAP(rAAAP)表现出特异性反应,rAAAP ELISA进一步证实了这一点,该方法还表明与感染牛无形体或绵羊和山羊其他相关病原体的动物血清无交叉反应。对5只实验感染绵羊进行为期1年的抗体动力学检测表明,rAAAP ELISA适用于检测绵羊无形体感染的早期和持续性感染。对中国23个省份54个地区采集的3138份野外血清样本进行调查发现,血清阳性率在9.4%至65.3%之间,这与先前关于绵羊无形体感染的报道一致。
鉴定出一种源自绵羊无形体的抗原蛋白AAAP,并证实了重组AAAP的抗原性。利用rAAAP建立了间接ELISA检测方法,该方法已被证明是调查绵羊和山羊绵羊无形体病流行情况的一种替代血清学诊断工具。